Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Stryker Orthopaedics Ball Impactor Tip Product Usage: Used for ADM Recalled by Stryker Howmedica Osteonics Corp. Due to Stryker has received complaints associated with cracks and/or...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Howmedica Osteonics Corp. directly.
Affected Products
Stryker Orthopaedics Ball Impactor Tip Product Usage: Used for ADM Surgery.
Quantity: 1,024 units
Why Was This Recalled?
Stryker has received complaints associated with cracks and/or fracture of the Ball Impactor Tip and Rim Impactor Tip Instruments.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Howmedica Osteonics Corp.
Stryker Howmedica Osteonics Corp. has 87 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report